Canonical Allele Identifier: CA2059449617
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855273A= , CM000674.2:g.102855273A= GRCh38
NC_000012.11:g.103249051A= , CM000674.1:g.103249051A= GRCh37
NC_000012.10:g.101773181A= NCBI36
NG_008690.1:g.67330T=
NG_008690.2:g.108138T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.569T= MANE Select ENSP00000448059.1:p.Val190=
ENST00000307000.7:c.554T= ENSP00000303500.2:p.Val185=
ENST00000549111.5:n.665T=
ENST00000553106.5:c.569T= ENSP00000448059.1:p.Val190=
NM_000277.1:c.569T= NP_000268.1:p.Val190=
XM_011538422.1:c.569T= XP_011536724.1:p.Val190=
NM_000277.2:c.569T= NP_000268.1:p.Val190=
NM_001354304.1:c.569T= NP_001341233.1:p.Val190=
XM_017019370.2:c.569T= XP_016874859.1:p.Val190=
NM_000277.3:c.569T= MANE Select NP_000268.1:p.Val190=
NM_001354304.2:c.569T= NP_001341233.1:p.Val190=